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MDR event

Received Jul 30, 2024

Report COR24000151-000 · MDR key 19876629

Device

Product problems

Device Operational Issue
Device Operational Issue

Patient

NA

inforMED sources data from the FDA's public MAUDE, recall, 510(k), and registration & listing databases via openFDA.

Not affiliated with the FDA. Data is unvalidated and may be incomplete — verify anything decision-critical against the source database.